International safety notice

Expanded Recall concerning Vitrea Z-Axis Measurement Error on Vitrea software versions, Vital Images

Germany / BfArM · DEU · May 10, 2013

Key facts

Title Expanded Recall concerning Vitrea Z-Axis Measurement Error on Vitrea software versions, Vital Images
Regulator Germany / BfArM
Country DEU
Brand Expanded Recall concerning Vitrea Z-Axis Measurement Error on Vitrea software versions, Vital Images
Manufacturer Expanded Recall concerning Vitrea Z-Axis Measurement Error on Vitrea software versions, Vital Images
Models 6.3.0, 6.3.2, 6.1.6, 1-800-208-3005, 6.2.3, 952-540-3717, EU13VI_A, NON-90
Date May 10, 2013
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices